EP2228487B1 - Zusammensetzung zur Polyestergewebebehandlung - Google Patents

Zusammensetzung zur Polyestergewebebehandlung Download PDF

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Publication number
EP2228487B1
EP2228487B1 EP10154216A EP10154216A EP2228487B1 EP 2228487 B1 EP2228487 B1 EP 2228487B1 EP 10154216 A EP10154216 A EP 10154216A EP 10154216 A EP10154216 A EP 10154216A EP 2228487 B1 EP2228487 B1 EP 2228487B1
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Prior art keywords
monomer
composition
acids
meth
acid salts
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EP10154216A
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English (en)
French (fr)
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EP2228487A1 (de
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Stephanie Nussbaum Cottrell
Tirthankar Ghosh
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Rohm and Haas Co
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Rohm and Haas Co
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    • D—TEXTILES; PAPER
    • D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M11/00—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with inorganic substances or complexes thereof; Such treatment combined with mechanical treatment, e.g. mercerising
    • D06M11/83—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with inorganic substances or complexes thereof; Such treatment combined with mechanical treatment, e.g. mercerising with metals; with metal-generating compounds, e.g. metal carbonyls; Reduction of metal compounds on textiles
    • D—TEXTILES; PAPER
    • D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M15/00—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
    • D06M15/19—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with synthetic macromolecular compounds
    • D06M15/21—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N59/00—Biocides, pest repellants or attractants, or plant growth regulators containing elements or inorganic compounds
    • A01N59/16—Heavy metals; Compounds thereof
    • D—TEXTILES; PAPER
    • D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M11/00—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with inorganic substances or complexes thereof; Such treatment combined with mechanical treatment, e.g. mercerising
    • D06M11/58—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with inorganic substances or complexes thereof; Such treatment combined with mechanical treatment, e.g. mercerising with nitrogen or compounds thereof, e.g. with nitrides
    • D—TEXTILES; PAPER
    • D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M13/00—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment
    • D06M13/10—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment with compounds containing oxygen
    • D06M13/184—Carboxylic acids; Anhydrides, halides or salts thereof
    • D06M13/207—Substituted carboxylic acids, e.g. by hydroxy or keto groups; Anhydrides, halides or salts thereof
    • D06M13/217—Polyoxyalkyleneglycol ethers with a terminal carboxyl group; Anhydrides, halides or salts thereof
    • D—TEXTILES; PAPER
    • D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M13/00—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment
    • D06M13/244—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment with compounds containing sulfur or phosphorus
    • D06M13/248—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment with compounds containing sulfur or phosphorus with compounds containing sulfur
    • D—TEXTILES; PAPER
    • D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M15/00—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
    • D06M15/19—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with synthetic macromolecular compounds
    • D06M15/37—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • D06M15/507—Polyesters
    • D—TEXTILES; PAPER
    • D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M15/00—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
    • D06M15/19—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with synthetic macromolecular compounds
    • D06M15/37—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • D06M15/55—Epoxy resins
    • D—TEXTILES; PAPER
    • D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M15/00—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
    • D06M15/19—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with synthetic macromolecular compounds
    • D06M15/37—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • D06M15/564—Polyureas, polyurethanes or other polymers having ureide or urethane links; Precondensation products forming them
    • D—TEXTILES; PAPER
    • D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M15/00—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
    • D06M15/19—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with synthetic macromolecular compounds
    • D06M15/37—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • D06M15/564—Polyureas, polyurethanes or other polymers having ureide or urethane links; Precondensation products forming them
    • D06M15/568—Reaction products of isocyanates with polyethers
    • D—TEXTILES; PAPER
    • D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M15/00—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
    • D06M15/19—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with synthetic macromolecular compounds
    • D06M15/37—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • D06M15/564—Polyureas, polyurethanes or other polymers having ureide or urethane links; Precondensation products forming them
    • D06M15/572—Reaction products of isocyanates with polyesters or polyesteramides
    • D—TEXTILES; PAPER
    • D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M16/00—Biochemical treatment of fibres, threads, yarns, fabrics, or fibrous goods made from such materials, e.g. enzymatic
    • D—TEXTILES; PAPER
    • D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M2101/00—Chemical constitution of the fibres, threads, yarns, fabrics or fibrous goods made from such materials, to be treated
    • D06M2101/16—Synthetic fibres, other than mineral fibres
    • D06M2101/30—Synthetic polymers consisting of macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • D06M2101/32—Polyesters
    • D—TEXTILES; PAPER
    • D10—INDEXING SCHEME ASSOCIATED WITH SUBLASSES OF SECTION D, RELATING TO TEXTILES
    • D10B—INDEXING SCHEME ASSOCIATED WITH SUBLASSES OF SECTION D, RELATING TO TEXTILES
    • D10B2331/00—Fibres made from polymers obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds, e.g. polycondensation products
    • D10B2331/04—Fibres made from polymers obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds, e.g. polycondensation products polyesters, e.g. polyethylene terephthalate [PET]

Definitions

  • the present invention relates to a composition useful for treating polyester fabric.
  • the composition contains a silver-polymer complex which is introduced into polyester a fabric with a polyester polyurethane and an epoxy resin to provide a treated fabric.
  • the problem addressed by this invention is to provide a composition that introduces a biocidal silver material to a fabric to provide a treated fabric resistant to removal of biocide by laundering.
  • the present invention is directed to a composition useful for treating polyester fabric.
  • the composition comprises: (a) a silver-containing copolymer comprising polymerized units of a monomer X and a monomer Y; wherein monomer X is an ethylenically unsaturated compound having a substituent group selected from an unsaturated or aromatic heterocyclic group having at least one nitrogen atom; and wherein monomer Y is an ethylenically unsaturated compound selected from carboxylic acids, carboxylic acid salts, carboxylic acid esters, organosulfuric acids, organosulfuric acid salts, sulfonic acids, sulfonic acid salts, phosphonic acids, phosphonic acid salts, vinyl esters, (meth)acrylamides, C 8 -C 20 aromatic monomers containing at least one exocyclic ethylenic unsaturation and combinations thereof; (b) an epoxy resin; and (c) a polyester polyurethane.
  • the invention is further
  • copolymer refers to polymers polymerized from at least two different monomers. All percentages herein are by weight, unless specified otherwise. Percentages of monomers are based on total copolymer weight.
  • aqueous as used herein and in the appended claims means water and mixtures composed substantially of water and water miscible solvents.
  • polyester fabric refers to a fabric comprising at least 40% polyester, alternatively at least 50% polyester, alternatively at least 60%, alternatively at least 70%, alternatively at least 80%, alternatively at least 90%.
  • (meth) refers to, for example, both acrylic and methacrylic; acrylate and methacrylate; acrylamide and methacrylamide; etc.
  • the glass transition temperature ("Tg") for the copolymers of the present invention may be measured by differential scanning calorimetry (DSC) taking the mid-point in the heat flow versus temperature transition as the Tg value.
  • DSC differential scanning calorimetry
  • the copolymer comprises at least 15 wt% of monomer X derived units. In some aspects of these embodiments, the copolymer comprises at least 20 wt% of monomer X derived units. In some aspects of these embodiments, the copolymer comprises at least 25 wt% of monomer X derived units. In some aspects of these embodiments, the copolymer comprises at least 30 wt% of monomer X derived units. In some aspects of these embodiments, the copolymer comprises at least 35 wt% of monomer X derived units, alternatively at least 40 wt%. In some aspects of these embodiments, the copolymer comprises no more than 60 wt% of monomer X derived units, alternatively no more than 55 wt%, alternatively no more than 50 wt%.
  • monomer X is selected from vinylimidazoles, vinylimidazo lines, vinylpyridines, vinylpyrroles, derivatives thereof and combinations thereof. In some aspects of these embodiments, monomer X is selected from vinylimidazoles, vinylpyridines, derivatives thereof and combinations thereof. In some aspects of these embodiments, monomer X is selected from N-vinylimidazole, 2-vinylpyridine, 4-vinylpyridine and combinations thereof. In some aspects of these embodiments, monomer X is N-vinylimidazole (VI).
  • monomer Y is selected from carboxylic acids, carboxylic acid salts, carboxylic acid esters, organosulfuric acids, organosulfuric acid salts, sulfonic acids, sulfonic acid salts, phosphonic acids, phosphonic acid salts, vinyl esters, (meth)acrylamides, C 8 -C 20 aromatic monomers containing at least one exocyclic ethylenic unsaturation and combinations thereof.
  • monomer Y is selected from carboxylic acids, carboxylic acid esters (e.g., alkyl (meth)acrylates), (meth)acrylamides, C 8 -C 20 aromatic monomers containing at least one exocyclic ethylenic unsaturation and combinations thereof.
  • monomer Y is selected from acrylic acid (AA), methacrylic acid, itaconic acid, maleic acid, fumaric acid, methyl (meth)acrylate, ethyl (meth)acrylate, propyl (meth)acrylate, isopropyl acrylate, n-butyl (meth)acrylate, isobutyl (meth)acrylate, 2-ethylhexyl (meth)acrylate, decyl (meth)acrylate, lauryl (meth)acrylate, stearyl (meth)acrylate, styrene, vinyltoluene, ⁇ -methylstyrene and combinations thereof.
  • monomer Y comprises at least one C 2 -C 8 alkyl (meth)acrylate, alternatively at least one C 2 -C 6 alkyl (meth)acrylate, alternatively n-butyl (meth)acrylate; alternatively Y comprises at least one C 2 -C 8 alkyl (meth)acrylate and at least one carboxylic acid, alternatively at least one C 2 -C 6 alkyl (meth)acrylate and at least one carboxylic acid, alternatively n-butyl (meth)acrylate and at least one carboxylic acid; alternatively Y comprises at least one C 2 -C 8 alkyl (meth)acrylate and (meth)acrylic acid, alternatively at least one C 2 -C 6 alkyl (meth)acrylate and (meth)acrylic acid, alternatively n-butyl (meth)acrylate and (meth)acrylic acid; alternatively monomer Y comprises n-butyl acrylate (BA)
  • the method uses a copolymer comprising polymerized units of a monomer X and a monomer Y; wherein the copolymer comprises at least 15 wt% of monomer X derived units; wherein monomer X is selected from vinylimidazoles, vinylimidazo lines, vinylpyridines, vinylpyrroles, derivatives thereof and combinations thereof; and wherein monomer Y is selected from carboxylic acids, carboxylic acid salts, carboxylic acid esters, organosulfuric acids, organosulfuric acid salts, sulfonic acids, sulfonic acid salts, phosphonic acids, phosphonic acid salts, vinyl esters, (meth)acrylamides, C 8 -C 20 aromatic monomers containing at least one exocyclic ethylenic unsaturation and combinations thereof.
  • the copolymer comprises no more than 5 wt% of units derived from ethylenically unsaturated monomer containing an epoxide function. In some aspects of these embodiments, the copolymer comprises no more than 1 wt% of units derived from ethylenically unsaturated monomer containing an epoxide function. In some aspects of these embodiments, the copolymer comprises no more than 0.5 wt% of units derived from ethylenically unsaturated monomer containing an epoxide function.
  • the copolymer comprises no more than 0.1 wt% of units derived from ethylenically unsaturated monomer containing an epoxide function. In some aspects of these embodiments, the copolymer comprises no more than 0.05 wt% of units derived from ethylenically unsaturated monomer containing an epoxide function.
  • the composition comprising a copolymer has a pH of at least 8, alternatively at least 8.5, alternatively at least 9. In some aspects of these embodiments, the composition has a pH no greater than 10.5, alternatively no greater than 10. In some aspects of these embodiments, the composition has a pH of 8.5-10.5. In some aspects of these embodiments, the composition has a pH of 9-10.
  • the composition comprises a latex copolymer which has at least 20 wt% solids. In some aspects of these embodiments, the latex copolymer comprises at least 25 wt% solids. In some aspects of these embodiments, the latex copolymer comprises at least 30 wt% solids.
  • the composition comprises from 35 to 55 wt% of polymerized units derived from monomer X and 35 to 55 wt% of polymerized units derived from monomer Y. In some aspects of these embodiments, the composition comprises from 40 to 50 wt% of polymerized units derived from monomer X and 40 to 50 wt% of polymerized units derived from monomer Y.
  • the composition comprises polymerized units derived from a crosslinker.
  • Crosslinkers suitable for use with the present invention include multi-ethylenically unsaturated monomers.
  • the crosslinker derived units are derived from crosslinker selected from 1,4-butanediol diacrylate; 1,4-butanediol dimethacrylate; 1,6-hexanediol diacrylate; 1,1,1-trimethylol propane triacrylate; 1,1,1-trimethylol propane trimethacrylate; allyl methacrylate; divinylbenzene; and N-allyl acrylamide.
  • the crosslinker derived units are derived from crosslinker selected from 1,1,1-trimethylol propane trimethacrylate.
  • the composition comprises 0.01 to 10 wt% (based on solids) crosslinker. In some aspects of these embodiments, the composition comprises 0.01 to 5 wt% (based on solids) crosslinker. In some aspects of these embodiments, the composition comprises 0.01 to 1 wt% (based on solids) crosslinker.
  • the copolymer comprises from 1 wt% to 50 wt% silver, based on total copolymer weight including silver, alternatively from 2 wt% to 40 wt%, alternatively from 3 wt% to 20 wt%, alternatively from 5 wt% to 15 wt%.
  • Silver is in the form of Ag(I) ion, which typically is introduced in the form of silver nitrate. Methods for preparation of the copolymer have been disclosed previously, e.g., in U.S. Pat. Appl. Pub. No. US 2005/0227895 .
  • additional copolymer is added which is not complexed with silver; and/or other amine compounds or polymers may be added.
  • the epoxy resin comprises at least a difunctional epoxy compound, i.e., a compound having at least two epoxy groups per molecule.
  • the epoxy resin comprises bis-glycidyl ethers or esters, triglycidyl isocyanurate, 1-epoxyethyl-3,4-epoxycyclohexane, vinylcyclohexene dioxide, diglycidyl esters of dicarboxylic acids, diglycidyl ethers of diols or polyols.
  • Suitable examples of bis- and tris-glycidyl esters and ethers include bisphenol A diglycidyl ether, diglycidyl adipate; 1,4-diglycidyl butyl ether; ethylene glycol diglycidic ether; glycidyl ethers of glycerol, erythritol, pentaerythritol, trimethylol propane and sorbitol; epoxy resorcinol ethers; and diglycidyl ethers of polyethylene glycols.
  • the epoxy resin comprises a polymer of glycidyl (meth)acrylates and/or allyl glycidyl ether.
  • the epoxy resin is present in an amount that results in a 0.1:1 to 10:1 1 ratio of equivalents epoxide:equivalents X monomer unit.
  • the ratio is at least 0.2:1, alternatively at least 0.3: 1, alternatively at least 0.5:1, alternatively at least 0.8:1.
  • the ratio is no more than 7:1, alternatively no more than 5: 1, alternatively no more than 4:1.
  • an amine curing agent in addition to the copolymer is used.
  • amine curing agents are well known in the art and are described, e.g., in WO 2005/080481 .
  • These curing agents include polyfunctional primary and secondary amines and some tertiary amines, including amine-containing polymers.
  • the polyester polyurethane contains polymerized residues of a polyester polyol and a diisocyanate.
  • the diisocyanate may be an aromatic diisocyanate, e.g., toluene diisocyanate (TDI), diphenyl methane diisocyanate (MDI), p-xylylene diisocyanate, tetramethylxylene diisocyanate, isomers thereof or mixtures thereof; or an aliphatic diisocyanate, e.g., 1,6-hexamethylene diisocyanate, hydrogenated methylenediphenyl diisocyanate (HMDI), ethylene diisocyanate, isophorone diisocyanate, cyclohexane-1,4-diisocyanate, or a mixture thereof.
  • TDI toluene diisocyanate
  • MDI diphenyl methane diisocyanate
  • MDI is preferred, especially a mixture of 4,4' and 2,4' isomers.
  • Preferred aliphatic diisocyanates include, e.g., 1,6-hexamethylene diisocyanate, hydrogenated methylenediphenyl diisocyanate (HMDI), isophorone diisocyanate and mixtures thereof.
  • Polyester polyols include, e.g., hydroxyl terminated products of polyhydric alcohols such as ethylene glycol, propylene glycol, diethylene glycol, neopentyl glycol, trimethylol propane, glycerol, pentaerythritol, 1,4-butanediol, 1,6-hexanediol, furan dimethanol, cyclohexane 1,6-dimethanol, diols made from dimethyl carbonate and any of the above polyhydric alcohols or mixtures thereof with polycarboxylic acids or lactones, especially dicarboxylic acids such as succinic acid, adipic acid, glutaric acid, phthalic acids and caprolactone.
  • polyhydric alcohols such as ethylene glycol, propylene glycol, diethylene glycol, neopentyl glycol, trimethylol propane, glycerol, pentaerythritol, 1,4-butanedio
  • Preferred polyester polyols include, e.g., those formed from adipic acid and diols selected from hexanediol, ethylene glycol, 1,4-butanediol, propylene glycol and cyclohexane-1,6-dimethylol.
  • Preferably polyhydric alcohols having more than two hydroxyl groups are present to the extent of no more than 2 wt% of the polyol, alternatively no more than 1 wt%, alternatively no more than 0.5 wt%.
  • the polyurethane has Mn from 10,000 to 100,000 and Mw from 200,000 to 2,000,000
  • the polyester polyurethane is an aliphatic polyester polyurethane, i.e., it contains polymerized residues of an aliphatic polyester polyol and an aliphatic diisocyanate.
  • the level of silver-containing copolymer in the bath solution was maintained at 181 ppm silver to provide 300 ppm of silver on the dried fabric.
  • the bath was made using tap water that was pH adjusted using 28% NH 4 OH to a pH of 9.5-9.9, prior to the addition of the silver-containing copolymer.
  • Other ingredients were added at appropriate levels - the solution was mixed using a standard air mixer until homogeneous.
  • the substrate to be treated was passed through the bath solution and then passed through two nips rolls to express excess solution.
  • the treated substrate is tentered and dried 2-3 min @ 149-163°C.
  • the treated, dried substrate is washed as noted, and then submitted for Ag content and/or efficacy testing.
  • Samples were prepared with a silver-containing copolymer which had 45 wt% BA monomer units, 45 wt% VI monomer units and 10% AA monomer units, and which contained 11% silver, and/or with the epoxy resins/polyurethanes indicated in the tables below added to the treatment water.
  • the amount of epoxy resin was measured in equivalents epoxy group/equivalent of VI unit in the silver-containing copolymer.
  • the fabric substrate used for the testing was 100% polyester knit fabric, 3.5 oz/yd 2 (125 g/m 2 ) basis weight.

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  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Textile Engineering (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Dentistry (AREA)
  • Environmental Sciences (AREA)
  • Pest Control & Pesticides (AREA)
  • Plant Pathology (AREA)
  • Health & Medical Sciences (AREA)
  • Agronomy & Crop Science (AREA)
  • General Health & Medical Sciences (AREA)
  • Wood Science & Technology (AREA)
  • Zoology (AREA)
  • Inorganic Chemistry (AREA)
  • Biochemistry (AREA)
  • General Chemical & Material Sciences (AREA)
  • Microbiology (AREA)
  • Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
  • Compositions Of Macromolecular Compounds (AREA)
  • Epoxy Resins (AREA)
  • Chemical Or Physical Treatment Of Fibers (AREA)

Claims (10)

  1. Zusammensetzung, verwendbar zur Behandlung von Gewebe, wobei die Zusammensetzung umfaßt:
    (a) ein silberhaltiges Copolymer, umfassend polymerisierte Einheiten eines Monomers X und eines Monomers Y, wobei Monomer X eine ethylenisch ungesättigte Verbindung mit einer Substituentengruppe ist, ausgewählt aus einer ungesättigten oder aromatischen heterocyclischen Gruppe mit mindestens einem Stickstoffatom, und wobei das Monomer Y eine ethylenisch ungesättigte Verbindung ist, ausgewählt aus Carbonsäuren, Carbonsäuresalzen, Carbonsäureestern, Organoschwefelsäuren, Organoschwefelsäuresalzen, Sulfonsäuren, Sulfonsäuresalzen, Phosphonsäuren, Phosphonsäuresalzen, Vinylestern, (Meth)acrylamiden, C8-C20 aromatischen Monomeren, enthaltend mindestens eine exocyclische ethylenische Ungesättigtheit, und Kombinationen davon,
    (b) ein Epoxyharz, und
    (c) ein Polyesterpolyurethan.
  2. Zusammensetzung gemäß Anspruch 1, wobei das Monomer X N-Vinylimidazol ist und das Monomer Y mindestens ein Alkyl(meth)acrylat umfaßt.
  3. Zusammensetzung gemäß Anspruch 2, wobei das Copolymer 5 Gew.-% bis 15 Gew.-% Silber, bezogen auf das Gesamtcopolymergewicht, umfaßt.
  4. Zusammensetzung gemäß Anspruch 3, wobei das Copolymer 35 bis 55 Gew.-% an Einheiten, abgeleitet von Monomer X, und 35 bis 55 Gew.-% an Einheiten, abgeleitet von Monomer Y, umfaßt.
  5. Zusammensetzung gemäß Anspruch 4, wobei das Monomer Y n-Butylacrylat und Acrylsäure umfaßt.
  6. Zusammensetzung gemäß Anspruch 3, wobei das Epoxyharz Trimethylolpropantriglycidylether ist und das Polyesterpolyurethan ein aliphatisches Polyesterpolyurethan ist.
  7. Verfahren zur Behandlung von Gewebe, wobei das Verfahren das Inkontaktbringen des Gewebes mit der Zusammensetzung gemäß Anspruch 1 umfaßt.
  8. Verfahren gemäß Anspruch 7, wobei das Monomer X N-Vinylimidazol ist und das Monomer Y mindestens ein Alkyl(meth)acrylat umfaßt.
  9. Verfahren gemäß Anspruch 8, wobei das Copolymer 5 Gew.-% bis 15 Gew.-% Silber, bezogen auf das Gesamtcopolyermergewicht, umfaßt.
  10. Verfahren gemäß Anspruch 9, wobei das Monomer Y n-Butylacrylat und Acrylsäure umfaßt.
EP10154216A 2009-03-11 2010-02-22 Zusammensetzung zur Polyestergewebebehandlung Not-in-force EP2228487B1 (de)

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JP2013129938A (ja) * 2011-12-21 2013-07-04 Komatsu Seiren Co Ltd 機能性繊維布帛及びその製造方法
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ES2358636T3 (es) 2011-05-12
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DE602010000006D1 (de) 2011-04-07
US7968619B2 (en) 2011-06-28
TW201035410A (en) 2010-10-01
KR20100102552A (ko) 2010-09-24
MX2010001943A (es) 2011-05-02
TWI410549B (zh) 2013-10-01
US20100234519A1 (en) 2010-09-16
CN101838935B (zh) 2012-11-28
CN101838935A (zh) 2010-09-22
BRPI1000652A2 (pt) 2011-03-22
JP2011012380A (ja) 2011-01-20
JP4910053B2 (ja) 2012-04-04
KR101099057B1 (ko) 2011-12-26

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